A Phase 1 Study of HLD-0117 in Patients With Estrogen Receptor Positive (ER+) Metastatic Breast Cancer (MBC)
Summary
Assessment of the safety and efficacy of HLD-0117 as monotherapy in patients with estrogen receptor positive (ER+) metastatic breast cancer (MBC) or locally advanced breast cancer that have progressed on prior systemic therapies.
Detailed description
This study is an open-label, dose-escalation and cohort expansion study evaluating the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and anti-tumor activity of oral single-agent, HLD-0117 in patients with ER+ MBC that have progressed after at least 1 prior systemic line of therapy. During dose escalation, patients will be enrolled into monotherapy cohorts using a Bayesian optimal interval (BOIN) design. Cohorts will enroll a minimum of three patients, with staggered enrollment between cohorts. Backfilling into dose levels determined to be safe may occur to further characterize tolerability and efficacy. The purpose of the study is to determine the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDEs) of HLD-0117 as a monotherapy.
Arms & interventions
- DrugHLD-0117
A treatment cycle consists of 28 days. Treatment may continue until disease progression or study discontinuation (withdrawal of consent, intercurrent illness, unacceptable adverse event or any other changes unacceptable for further treatment, etc.)
Outcome measures
Primary
Dose Limiting Toxicities (DLTs)
Frequency of dose-limiting toxicities (DLTs)
Time frame: 28 days
AEs, ECGs, Labs and Clinical Changes
Frequency and severity of adverse events (AEs) and abnormal electrocardiogram (ECG), laboratory and clinical changes from baseline
Time frame: 28 days
Secondary
Objective response rate (ORR)
Time frame: 56 Days
Duration of response (DOR)
Time frame: 28 days
Progression-free survival (rPFS)
Time frame: 56 days
Disease Control Rate (DCR)
Time frame: 24 weeks
Eligibility criteria
Study locations (4)
Yale- New Haven Hospital- Yale Cancer Center
New Haven, Connecticut, 06510
Florida Cancer Specialists
Sarasota, Florida, 34231
SCRI Oncology Partners
Nashville, Tennessee, 37203
NEXT Oncology
Fairfax, Virginia, 22031